A green and economic approach to synthesize magnetic Lagenaria siceraria biochar (γ-Fe2O3-LSB) for methylene blue removal from aqueous solution.

In the printing and textile industries, methylene blue (a cationic azo dye) is commonly used. MB is a well-known carcinogen, and another major issue is its high content in industrial discharge. There are numerous removal methodologies that have been employed to remove it from industrial discharge; however, these current modalities have one or more limitations. In this research, a novel magnetized biochar (γ-Fe2O3-LSB) was synthesized using Lagenaria siceraria peels which were further magnetized via the co-precipitation method. The synthesized γ-Fe2O3-LSB was characterized using FTIR, X-ray diffraction, Raman, SEM-EDX, BET, and vibrating sample magnetometry (VSM) for the analysis of magnetic properties. γ-Fe2O3-LSB showed a reversible type IV isotherm, which is a primary characteristic of mesoporous materials. γ-Fe2O3-LSB had a specific surface area (SBET = 135.30 m2/g) which is greater than that of LSB (SBET = 11.54 m2/g). γ-Fe2O3-LSB exhibits a saturation magnetization value (Ms) of 3.72 emu/g which shows its superparamagnetic nature. The batch adsorption process was performed to analyze the adsorptive removal of MB dye using γ-Fe2O3-LSB. The adsorption efficiency of γ-Fe2O3-LSB for MB was analyzed by varying parameters like the initial concentration of adsorbate (MB), γ-Fe2O3-LSB dose, pH effect, contact time, and temperature. Adsorption isotherm, kinetic, and thermodynamics were also studied after optimizing the protocol. The non-linear Langmuir model fitted the best to explain the adsorption isotherm mechanism and resulting adsorption capacity ( q e =54.55 mg/g). The thermodynamics study showed the spontaneous and endothermic nature, and pseudo-second-order rate kinetics was followed during the adsorption process. Regeneration study showed that γ-Fe2O3-LSB can be used up to four cycles. In laboratory setup, the cost of γ-Fe2O3-LSB synthesis comes out to be 162.75 INR/kg which is low as compared to commercially available adsorbents. The results obtained suggest that magnetic Lagenaria siceraria biochar, which is economical and efficient, can be used as a potential biochar material for industrial applications in the treatment of wastewater.

An Asymmetric Coumarin-Anthracene Conjugate as Efficient Fullerene-Free Acceptor for Organic Solar Cells.

Asymmetric wide-bandgap fullerene-free acceptors (FFAs) play a crucial role in organic solar cells (OSCs). Here, we designed and synthesized a simple asymmetric coumarin-anthracene conjugate named CA-CN with optical bandgap of 2.1 eV in a single-step condensation reaction. Single crystal X-ray structure analysis confirms various multiple intermolecular non-covalent interactions. The molecular orbital energy levels of CA-CN estimated from cyclic voltammetry were found to be suitable for its use as an acceptor for OSCs. Binary OSCs fabricated using CA-CN as acceptor and PTB7-Th as the donor achieve a power conversion efficiency (PCE) of 11.13%. We further demonstrate that the insertion of 20 wt% of CA-CN as a third component in ternary OSCs with PTB7-Th:DICTF as the host material achieved an impressive PCE of 14.91%, an improvement of ~43% compared to the PTB7-Th:DICTF binary device (10.38%). Importantly, the ternary blend enhances the absorption coverage from 400 to 800 nm and improves the morphology of the active layer. The findings highlight the efficacy of an asymmetric design approach for FFAs, which paves the way for developing high-efficiency OSCs at low cost.

Impact of high energy photons on physical, structural and magnetic properties of Mn0.65Zn0.35Fe2-xNdxO4 nanoparticles.

Ultrafine powders of Nd+3 doped Mn-Zn ferrite powders with composition Mn0.65Zn0.35Fe2-xNdxO4 (x = 0.04, 0.06, 0.08) were prepared using the combustion method of preparation. Monophasic nanoparticle formation was confirmed by X-ray diffraction. The particle size was determined using a Transmission electron microscope (TEM). The nanopowders were investigated for their physical, structural, and magnetic properties and then radiated with gamma photons obtained from Co60 source with a dose of 500Gy, 750Gy and 1000Gy. The characterization of radiated powders showed preservation of spinel structure with breaking down of crystallites into finer crystals with increment in amorphous content. Structural and physical parameters were drastically altered due to high-energy photon exposure. The breaking down of larger particles was observed as a result of photon energy impact on the samples. The Saturation magnetization of ferrite nanoparticles was observed to increase with increasing gamma radiation dose. Mössbaure spectra showed the dominance of Fe+3 in the high spin state.

Effects of Halogenation on Cyclopentadithiophenevinylene-Based Acceptors with Excellent Responses in Binary Organic Solar Cells.

In recent years, non-fused non-fullerene acceptors (NFAs) have attracted increasing consideration due to several advantages, which include simple preparation, superior yield, and low cost. In the work reported here, we designed and synthesized three new NFAs with the same cyclopentadithiophenevinylene (CPDTV) trimer as the electron-donating unit and different terminal units (IC for FG10, IC-4F for FG8, and IC-4Cl for FG6). Both halogenated NFAs, i.e., FG6 and FG8, show red-shifted absorption spectra and higher electron mobilities (more pronounced for FG6) in comparison with FG10. Moreover, the dielectric constants of these materials also increased upon halogenation of the IC terminal units, thus leading to a reduction in the exciton binding energy, which is favorable for dissociation of excitons and subsequent charge transfer despite the driving force (highest occupied molecular orbital and lowest unoccupied molecular orbital offsets) being very small. The organic solar cells (OSCs) constructed using these acceptors and PBDB-T, as the donor, showed PCE values of 15.08, 12.56, and 9.04% for FG6, FG8, and FG10, respectively. The energy loss for the FG6-based device was the lowest (0.45 eV) of all the devices, and this may be attributed to it having the highest dielectric constant, which leads to a reduction in the binding energy of exciton and a small driving force for hole transfer from FG6 to PBDB-T. The results indicate that the NFA containing the CPDTV oligomer core and halogenated terminal units can efficiently spread the absorption spectrum to the NIR zone. Non-fused NFAs have a bright future in the quest to obtain efficient OSCs with low cost for marketable purposes.

Impact of gadolinium doping into the frustrated antiferromagnetic lithium manganese oxide spinel.

Cubic spinel LiMn2O4 (LMO) are promising electrode materials for advanced technological devices owing to their rich electrochemical properties. Here, a series of Gd3+-doped LiMn2O4 were synthesized using a simple one-step sol-gel synthesis, and a systematized study on the effect of increasing Gd3+ concentration on magnetic properties is conferred. The Raman and density functional theory (DFT) calculations of the synthesized materials were correlated with the magnetic properties; we observed a high coercivity value for the doped LMO compared to pristine LMO, which scales down from 0.57T to 0.14T with an increase in Gd concentration. The samples exhibited paramagnetic (at 300K) to antiferromagnetic (at 5K) transition and variation in the magnetic moment due to the replacement of Mn+2 or Mn+3 ion by Gd+3 ion from the octahedral 16d lattice site. The observed phase transitions in the hysteresis curve below the Neel temperature (TN) at 5K are found to be due to the superexchange mechanism.

Luminescence studies of binding affinity of vildagliptin with bovine serum albumin.

Vildagliptin (VDG)is a frontier drug for diabetes mellitus. It is prescribed both in the monotherapy as well as in an amalgamation with other antidiabetic drugs. Drug-serum protein binding is an essential parameter which influences ADME properties of the drug. In current study, binding of VDG with serum protein (bovine serum albumin: BSA) was investigated using multi-spectroscopic techniques. A computational approach was also employed to identify the binding affinity of VDG with BSA at both Sudlow I and II sites. An enzyme activity assay specific for esterase was also investigated to know the post-binding consequences of VDG with BSA. Fluorescence spectra of BSA samples treated with VDG shows static quenching with binding parameters for VDG-BSA complex show single class of equivalent binding stoichiometry(n = 1.331) and binding constant 1.1 x 104M-1 at 298.15 K. The binding constant indicates important role of non-polar interactions in the binding process. Fluorescence resonance energy transfer (FRET) analysis of VDG absorption spectra and emission spectrum of BSA confirmed no significant resonance in energy transfer. Synchronous fluorescence of BSA after binding with VDG show maximum changes in emission intensity at tryptophan (Trp) residues. Post binding with VDG, BSA conformation changes as suggested by circular dichorism (CD) spectra of BSA and this lead to enhanced protein stability as indicated by a thermal melting curve of BSA.Communicated by Ramaswamy H. Sarma.

Microstructural tuning and band gap engineering of calcium hydroxides: a novel approach by pH variation.

Here we report a simple, inexpensive, energy benign, yet novel pH-driven chemical precipitation technique to achieve microstructural and band gap engineering of calcium hydroxide nanoparticles (CHNPs). The chemical precipitation route involved the use of 0.4-1.6 M Ca(NO3 )2 .4H2 O solutions as the precursor and 1 M NaOH solution as the precipitator. The simple variation in precursor molarity induces a pH change from about 12.4 to 11.3 in the reactant solution. The CHNPs characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR), dynamic light scattering (DLS), and ultraviolet-visible (UV-Vis) spectroscopy techniques confirm a jump of nanocrystallite size from ~50-70 nm with a concomitant reduction of direct optical band gap energy from ~5.38-5.26 eV. The possible mechanisms that could be operative behind obtaining microstructurally tuned (MT)-CHNPS and band gap engineering (BGE) are discussed from both theoretical and physical process perspectives. Furthermore, the implications of these novel results for possible futuristic applications are briefly hinted upon.

Optical band gap enhancements of chemically synthesized α-Ni(OH)2 nanoparticles by a novel technique: Precipitator molarity variation.

Nickel hydroxide nanoparticles (NHNPs) are extremely important semiconducting materials for applications in energy storage and energy harvesting devices. This study uses a novel variation in molarity of the sodium hydroxide (NaOH) precipitator solution to enhance the direct optical band gap in the NHNPs chemically synthesized by using nickel nitrate hexahydrate (Ni(NO3 )2 ·6H2 O) as the precursor. The simple, energy benign chemical precipitation route involved the usage of 1 M (Ni(NO3 )2 ·6H2 O) solutions as the precursor and 0.4 M, 0.6 M, and 0.8 M NaOH solutions as the precipitator solutions. The simple variation in precipitator molarity induces an increase in pH from about 6.9 to 7.5 of the reactant solution. As the molarity of the precursor solution does not change, the change in pH of the reactant solution is equivalent to the change in the pH of the precipitator solution. The NHNPs characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), dynamic light scattering (DLS), Fourier-transform infrared (FTIR) and ultraviolet-visible (UV-vis) techniques confirm a reduction of the nanocrystallite size from about 6.8 to 4.5 nm with a concomitant enhancement in the direct optical band gap energy from about 2.64 to 2.74 eV. The possible mechanisms that could be operative behind obtaining microstructurally tuned (MT)-NHNPs and band gap engineering (BGE) of the MT-NHNPs are discussed from both theoretical and physical process perspectives. Further, the implications of these novel results for possible future applications are briefly touched upon. The reported results might be useful to assess the material as an active electrode to improve the performance of batteries.

Waste Citrus reticulata Assisted Preparation of Cobalt Oxide Nanoparticles for Supercapacitors.

The green, sustainable, and inexpensive creation of novel materials, primarily nanoparticles, with effective energy-storing properties, is key to addressing both the rising demand for energy storage and the mounting environmental concerns throughout the world. Here, an orange peel extract is used to make cobalt oxide nanoparticles from cobalt nitrate hexahydrate. The orange peel extract has Citrus reticulata, which is a key biological component that acts as a ligand and a reducing agent during the formation of nanoparticles. Additionally, the same nanoparticles were also obtained from various precursors for phase and electrochemical behavior comparisons. The prepared Co-nanoparticles were also sulfurized and phosphorized to enhance the electrochemical properties. The synthesized samples were characterized using scanning electron microscopic and X-ray diffraction techniques. The cobalt oxide nanoparticle showed a specific capacitance of 90 F/g at 1 A/g, whereas the cobalt sulfide and phosphide samples delivered an improved specific capacitance of 98 F/g and 185 F/g at 1 A/g. The phosphide-based nanoparticles offer more than 85% capacitance retention after 5000 cycles. This study offers a green strategy to prepare nanostructured materials for energy applications.

TiO2 based Photocatalysis membranes: An efficient strategy for pharmaceutical mineralization.

Among the various emerging contaminants, pharmaceuticals (PhACs) seem to have adverse effects on the quality of water. Even the smallest concentration of PhACs in ground water and drinking water is harmful to humans and aquatic species. Among all the deaths reported due to COVID-19, the mortality rate was higher for those patients who consumed antibiotics. Consequently, PhAC in water is a serious concern and their removal needs immediate attention. This study has focused on the PhACs' degradation by collaborating photocatalysis with membrane filtration. TiO2-based photocatalytic membrane is an innovative strategy which demonstrates mineralization of PhACs as a safer option. To highlight the same, an emphasis on the preparation and reinforcing properties of TiO2-based nanomembranes has been elaborated in this review. Further, mineralization of antibiotics or cytostatic compounds and their degradation mechanisms is also highlighted using TiO2 assisted membrane photocatalysis. Experimental reactor configurations have been discussed for commercial implementation of photoreactors for PhAC degradation anchored photocatalytic nanomembranes. Challenges and future perspectives are emphasized in order to design a nanomembrane based prototype in future for wastewater management.

Modeling nonlinear high-pressure sensors based on degenerate four-wave mixing in photonic crystal fibers.

We propose a high-pressure sensing mechanism in solid-core silica photonic crystal fibers (PCF) that is based on the nonlinear optical process of degenerate four-wave mixing. A quite simple configuration for the pressure sensor is given and is theoretically investigated by obtaining signal gain spectra. We focus on the Stokes and anti-Stokes sidebands that are generated during propagation of the field along the PCF due to the interplay of dispersion and nonlinear optical effects. We have considered wave propagation in the normal dispersion regime with the inclusion of negative fourth-order dispersion. We have also considered a pumping field with wavelength of 1076 nm and peak power of 3000 W that propagates along a PCF with 40 cm of length. We have optimized sensitivity, varying lattice pitch and air-hole diameter, and we have obtained high sensitivities of the Stokes and anti-Stokes lines of 3.672 and -0.146nm/MPa, respectively. The proposed sensors have potential applicability in high-pressure environments.

New Medium Bandgap Donor D-A1 -D-A2 Type Copolymers Based on Anthra[1,2-b: 4,3-b":6,7-c"'] Trithiophene-8,12-dione Groups for High-Efficient Non-Fullerene Polymer Solar Cells.

A new acceptor unit anthra[1,2-b: 4,3-b': 6,7-c'']trithiophene-8,12-dione (А3Т) (A2) is synthesized and used to design D-A1 -D-A2 medium bandgap donor copolymers with same thiophene (D) and A2 units but different A1, i.e., fluorinated benzothiadiazole (F-BTz) and benzothiadiazole (BTz) denoted as P130 and P131, respectively. Their detailed optical and electrochemical properties are examined. The copolymers show good solubility in common organic solvents, broad absorption in the visible spectral region from 300 to 700 nm, and deeper HOMO levels of -5.45 and -5.34 eV for P130 and P131, respectively. Finally, an optimized polymer solar cell (PSC) based on P131 as the donor and narrow bandgap non-fullerene small molecule acceptor Y6 demonstrated a power conversion efficiency (PCE) of >11.13%. To further improve the efficiency of the non-fullerene PSC, the P130 is optimized by introducing a fluorine atom into the BTz unit, F-BTz acceptor unit, and PCE PSC based on P130: Y6 active layer increased to >15.28%, which is higher than that for the non-fluorinated analog P131:Y6. The increase in the PCE for former PSC is attributed to the more crystalline nature and compact π-π stacking distance, leading to more balanced charge transport and reduced charge recombination. These remarkable results demonstrate that A3T-based copolymer P130 with F-BTz as the second acceptor is a promising donor material for high-performance PSCs.

Fullerene/Non-fullerene Alloy for High-Performance All-Small-Molecule Organic Solar Cells.

Organic solar cells (OSCs) that contain small molecules only were prepared with FG1 as the donor, a narrow band gap non-fullerene acceptor MPU4, and a wide band gap PC71BM. The OSCs based on optimized FG1:MPU4 (1:1.2) and FG1:PC71BM (1:1.5) active layers, respectively, gave power conversion efficiencies (PCEs) of 11.18% with a short circuit current (JSC) of 19.54 mA/cm2, open circuit voltage (VOC) of 0.97 V, and fill factor (FF) of 0.59, and 6.62% with a JSC of 12.50 mA/cm2, VOC of 0.84 V, and FF of 0.63%, respectively. A PCE of 13.26% was obtained from the optimized ternary FG1:PC71BM:MPU4 (1:0.3:0.9) OSCs and this arises because of the boost in a JSC of 21.91 mA/cm2 and FF of 0.68. The VOC of the ternary OSCs (0.89 V) lies between those for the OSCs based on FG1:MPU4 and FG1:PC71BM, which indicates the formation of an alloy of the two acceptors. The increase in JSC and FF in the ternary OSCs may result from the efficient energy transfer from PC71BM to MPU4 as well as more charge-transfer donor/acceptor interfaces, enhanced charge carrier mobilities resulting in better adjusted charge transport, and lower bimolecular and trap-assisted recombination. The appropriate phase separation, increased crystallinity, and reduced π-π stacking distance in the ternary active layer are consistent with the enhancement in the FF for OSCs based on a ternary active layer. The results of this work suggest the merging of the fullerene acceptor into the non-fullerene acceptor to form a fullerene/non-fullerene acceptor alloy, and this may be a viable approach to obtain high-performance OSCs.

Reducing Energy Loss in Organic Solar Cells by Changing the Central Metal in Metalloporphyrins.

The effect of central donor core on the properties of A-π-D-π-A donors, where D is a porphyrin macrocycle, cyclopenta[2,1-b:3,4-b']dithiophene is the π bridge, and A is a dicyanorhodanine terminal unit, was investigated for the fabrication of the organic solar cells (OSCs), along [6,6]-phenyl-C71-butyric acid methyl ester (PC71 BM) as electron acceptor. A new molecule consisting of Ni-porphyrin central donor core (VC9) showed deep HOMO energy level and OSCs based on optimized VC9:PC71 BM realized overall power conversion efficiency (PCE) of 10.66 % [short-circuit current density (JSC )=15.48 mA/cm2 , fill factor (FF)=0.65] with high open circuit voltage (VOC ) of 1.06 V and very low energy loss of 0.49 eV, whereas the Zn-porphyrin analogue VC8:PC71 BM showed PCE of 9.69 % with VOC of 0.89 V, JSC of 16.25 mA/cm2 and FF of 0.67. Although the OSCs based on VC8 showed higher JSC in comparison to VC9, originating from the broader absorption profile of VC8 that led to more exciton generation, the higher value of PCE of VC9 is owing to the higher VOC and reduced energy loss.

Edge plane pyrolytic graphite as a sensing surface for the determination of fluvoxamine in urine samples of obsessive-compulsive disorder patients.

There is an increasing demand for fast and sensitive determination of antidepressants in human body fluids because of the present scenario of rising depression cases at the global level. A simple and sensitive voltammetric method using edge plane pyrolytic graphite electrode (EPPGE) as a novel sensor is presented for the determination of antidepressant fluvoxamine in urine and blood plasma samples of obsessive-compulsive disorder (OCD) patients. EPPGE is delineated the first time for this determination. EPPGE exhibited strong electrocatalytic activity and enhanced reduction signal towards the sensing of fluvoxamine. Fluvoxamine gave a well-defined reduction peak at ~ - 670 mV using EPPGE. The fluvoxamine reduction peak current was linear to its concentration in the range 5.00 × 10-9 - 0.1 × 10-6 mol L-1 and the limit of detection was found to be 3.5 × 10-9 mol L-1. The pre-eminence of EPPGE over mercury electrodes has been proved in terms of sensitivity and imperative analytical parameters. The pH study reveals the involvement of an equal number of electrons and protons in the reduction reaction mechanism. The frequency study indicated the adsorption controlled irreversible reaction mechanism. The stability and reproducibility of the offered sensor were also found most favorable. The interference study confirmed the optimum selectivity of the proposed sensor. The edge plane pyrolytic graphite sensing platform is recommended as a potential contender for the accurate and fast determination of fluvoxamine in depression medications as well as biological specimens of OCD patients.

Efficient Fullerene-Free Organic Solar Cells Using a Coumarin-Based Wide-Band-Gap Donor Material.

In recent years, tremendous growth has been seen for solution-processed bulk heterojunction solar cells (BHJSCs) using fullerene-free molecular acceptors. Herein, we report the synthesis, characterization of a coumarin-based organic semiconducting molecule C1, and its use in BHJSCs as an electron donor. The compound exhibited an absorption band at 472 nm in chloroform solution with an optical energy gap of 2.33 eV. The HOMO/LUMO energy levels of C1 were found to be ideal for use in BHJSCs. Using PC71BM and a fullerene-free acceptor IT-4F, the device generated power conversion efficiencies (PCEs) of 6.17 and 8.31%, respectively. The success of the device based on a fullerene-free acceptor is a result of complementary absorption and well-matched energy levels, resulting in an improved photocurrent and photovoltage in the device. Moreover, ternary solar cells fabricated by employing C1 (20 wt%) as a secondary donor, i.e., an active layer of C1:PM6:IT-4F (0.2:0.8:1.5), generated an enhanced PCE of 11.56% with a high short-circuit current density (JSC) of 16.42 mA cm-2, an open-circuit voltage (VOC) of 1.02 V, and a fill factor of 0.69 under 1 sun spectral illumination, which is ∼8% higher than that for the PM6:IT-4F-based binary device (PCE = 10.70%). The increased PCE for the ternary organic solar cell may be related to the efficient exciton generation and its dissociation via Forster resonance energy transfer, which guarantees enough time for an exciton to diffuse toward the D/A interfaces.

Nano-scale depth-varying recrystallization of oblique Ar+ sputtered Si(111) layers.

Silicon, the workhorse of semiconductor industry, is being exploited for various functional applications in numerous fields of nanotechnology. In this paper, we report the fabrication of depth controllable amorphous silicon (a-Si) layers under 80 keV Ar+ ion sputtering at off-normal ion incidences of 30°, 40° and 50° and crystallization of these amorphous Si(111) layers under thermal annealing. We find that the irradiated samples were not fully amorphized even for the lowest oblique incidence of 30°. Sputtering at off-normal incidences induces depth controllable surface amorphization in Si(111). Annealing at temperature of 1,073 K is characterized by formation of depth-varying buried amorphous layer due to defect recrystallization and damage recovery. Some remnant tensile stress has been observed for recrystallized samples even for lowest oblique incidence. The correlation of amorphization and stress due to sputtering induced by oblique incidence has been discussed systematically. The possible mechanism of recrystallization is discussed in terms of vacancies produced in sputtering dominated regime and their migration during annealing treatment. Our results reveal that with appropriate selection of oblique ion beam sputtering parameters, depth controllable surface amorphization and recrystallization may be fine-tuned to achieve co-existing amorphous and crystalline phases, playing a crucial role in fabrication of substrates for IC industry.

Electrical transport properties of InAs nanowires synthesized by a solvothermal method.

Nanowires are widely considered to be key elements in future disruptive electronics and photonics. This paper presents the first detailed study of transport mechanisms in single-crystalline InAs nanowires synthesized by a cheap solvothermal wet chemical method. From detailed analyses of temperature-dependent current-voltage characteristics, it was observed that contacted nanowires operate in a linear transport regime at biases below a critical cross-over voltage. For larger biases, the transport changes to space-charge-limited conduction assisted by traps. The characteristic parameters such as free electron concentration, trap concentration and energy distribution, and electron mobility were all calculated. It was demonstrated that the nanowires have key electrical properties comparable to those of InAs nanowires grown by molecular beam epitaxy. Our results might pave the way for cheap disruptive low-dimensional electronics such as resistive switching devices.

Nanoscale structural defects in oblique Ar+ sputtered Si(111) surfaces.

The present endeavor investigates the controlled surface modifications and evolution of self-assembled nano-dimensional defects on oblique Ar+ sputtered Si(111) surfaces which are important substrates for surface reconstruction. The defect formation started at off-normal incidences of 50° and then deflates into defined defect zones with decrease in oblique incidence, depending strongly on angle of ion incidence. Interestingly, it is observed that mean size & height decreases while average density of these defects increases with decreasing oblique incidence. Non-linear response of roughness of irradiated Si(111) with respect to oblique incidence is observed. Crystalline (c-Si) to amorphous (a-Si) phase transition under oblique argon ion irradiation has been revealed by Raman spectroscopy. Our analysis, thus, shows that high dose argon ion irradiation generates of self-assembled nano-scale defects and surface vacancies & their possible clustering into extended defect zones. Explicitly, ion beam-stimulated mass transport inside the amorphous layers governs the observed defect evolution. This investigation of crystalline (c-Si) coupled with amorphous (a-Si) phases of nano-structured surfaces provides insight into the potential applications in the nano-electronic and optoelectronic devices thus, initiating a new era for fabricating multitude of novel structures.

Self-assembled nano-dots structures on Si(111) surfaces by oblique angle sputter-deposition.

Controlled surface modification and nano-dots structures over Si(111) surfaces have been produced by oblique angle sputter deposition of 80 keV Ar+ beam. Temporal parameters such as self-assemble, tunability of size and density of fabricated nano-dots exhibit distinct fluence dependence. Crystalline to amorphous (c/a) phase transition for sputter deposited Si(111) surfaces has been observed. RBS/C reveals the non-linear response of damage distribution with Ar ion fluence. Compositional alterations like degree of amorphization, damage distribution and depth profiling of Ar in these nano-structured surfaces has been correlated with the morphological and structural findings. The underlying self-organization mechanism relies in ion beam sputtering induced erosion and re-deposition of Si atoms thereby leading to mass transport inside the amorphous layers. Such nano-structured Si(111) surfaces could be applied as key engineering substrates for surface reconstruction, optoelectronic devices, data storage devices, recording media and photovoltaic applications.